Canonical Allele Identifier: PA167873
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 92576
ClinVar RCV Id: RCV000168135 RCV000131252 RCV000217757 RCV000679234 RCV001083147 RCV001356423
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg1068Gln
CA011934
NM_000179.3:c.3203G>A